Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
Endocrinologia, Diabetes Y Nutricion|April 21, 2019
SEEN guidelines for the management and prevention of acute adrenal insufficiencyMarta Araujo Castro, María Currás Freixes, Paz de Miguel Novoa, et al.Nutricion Hospitalaria|July 11, 2022
[Benefits of telematic monitoring for weight loss in overweight and obese patients in times of confinement]Isabel Higuera Pulgar, Isabel Yagüe Lobo, Elena Sánchez Campayo, et al.Cancer Genetics|May 23, 2016
ATRX driver mutation in a composite malignant pheochromocytomaIñaki Comino-Méndez, Águeda M Tejera, María Currás-Freixes, et al.Cells|December 24, 2021
Alterations in SLC4A2, SLC26A7 and SLC26A9 Drive Acid-Base Imbalance in Gastric Neuroendocrine Tumors and Uncover a Novel Mechanism for a Co-Occurring Polyautoimmune ScenarioOriol Calvete, José Reyes, Hernán Valdés-Socin, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 20, 2017
Targeted Exome Sequencing of Krebs Cycle Genes Reveals Candidate Cancer-Predisposing Mutations in Pheochromocytomas and ParagangliomasLaura Remacha, Iñaki Comino-Méndez, Susan Richter, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 2, 2016
Targeted Sequencing Reveals Low-Frequency Variants in <i>EPHA</i> Genes as Markers of Paclitaxel-Induced Peripheral NeuropathyMaría Apellániz-Ruiz, Héctor Tejero, Lucía Inglada-Pérez, et al.Cancers|October 14, 2022
A Large Case-Control Study Performed in Spanish Population Suggests That <i>RECQL5</i> Is the Only RECQ Helicase Involved in Breast Cancer SusceptibilityErik Michel Marchena-Perea, Milton Eduardo Salazar-Hidalgo, Alicia Gómez-Sanz, et al.Journal of Molecular Medicine (Berlin, Germany)|June 14, 2015
Functional and in silico assessment of MAX variants of unknown significanceIñaki Comino-Méndez, Luis J Leandro-García, Guillermo Montoya, et al.Journal of the National Cancer Institute|March 14, 2015
Whole-exome sequencing identifies MDH2 as a new familial paraganglioma geneAlberto Cascón, Iñaki Comino-Méndez, María Currás-Freixes, et al.Database : the Journal of Biological Databases and Curation|July 5, 2024
SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish populationJosé M Moreno-Cabrera, Lidia Feliubadaló, Marta Pineda, et al.Pageof 1